INTRODUCING MASTERMIND 3.0
Mastermind’s new Gene Information Page puts comprehensive gene information and ACMG gene-wide parameters for interpretation of variants in large panels/whole exomes/genomes at your fingertips, so you can find the answers you need from just one platform.
Integrating Mastermind within our interpretation platform helps our users minimize the manual effort it takes to select and read relevant evidence-based papers.
Using Mastermind enhances our ability to provide clinicians at the bedside with important relevant information about known treatments and interventions.
Mastermind’s Supplemental data feature directly benefits my quality of life as a Variant Scientist.
I can say with certainty that without the findings obtained from Genomenon, I would not have been able to provide a diagnosis for this patient.
Genomenon’s methodology improved the efficiency and completeness of our literature review process.
I don’t consider a patient’s report complete unless every variant has been researched through Mastermind
Mastermind is the most exhaustive genomic knowledge base in existence, built by indexing nearly seven million full-text genomic articles and 500,000 supplemental data sets.
(Searching Mastermind by phenotype) will be invaluable in our ongoing work to diagnose and treat babies with rare diseases.